
Pharma RP & Quality Coordinator
- Op locatie
- Schiphol-Rijk, Noord-Holland, Nederland
- € 4.627 - € 6.010 per maand
- QESH
Functieomschrijving
What does the of Pharma RP & Quality Coordinator position entail:
In this role you are designated by management with authority to deal with pharmaceutical and healthcare related business.
You have authority to plan and coordinate implementation of the quality control over handling standards for pharmaceutical shipments within the organization.
Within this role you have authority for implementation of changes on QMS design, content and maintenance for continuous compliance and effectiveness.
Additionally, you have authority to delegate or coordinate your assignments to clearly defined delegated function or backup such us deputy, key or competent personnel or function with appropriate level of knowledge and training, related to pharmaceutical and healthcare business. During delegation you always remain accountable and responsible for the assignment and results.
Vereisten
What qualities do we need:
Relevant pharmacy / science-based qualification (ideally pharmacy, pharmaceutical sciences)
The prior relevant knowledge and experience related to the distribution of medicinal products
If not pharmacist or QA, at least one year of relevant practical and/or managerial experience of medicinal products
In addition, you have knowledge of:
The role of organizations that regulate those supplying medicinal products such as EMA, IGJ
The EU falsified Medicine Directive
The principles and guidelines of Good Distribution Practice and how the principles of GDP maintain product quality throughout the distribution chain
You have:
Understanding of the role and authority of the EMA and IGJ
Understanding of the EU and NL regulations in relation to Wholesale Distribution
Minimum 5 years' experience within a Pharmacy operational environment with key knowledge of the EMA / EU GDP Guidelines 2013/C 343/01 dated 05 November 2013 and latest IATA CEIV Pharma requirements and guidelines
Drug identification, specification and storage requirements
An awareness of European Guidelines on Good Practice of Medicinal Products'
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